S
Sherrie Secunda
Researcher at National Institutes of Health
Publications - 9
Citations - 442
Sherrie Secunda is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Adenosine receptor & Adenosine. The author has an hindex of 9, co-authored 9 publications receiving 428 citations.
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Journal ArticleDOI
An uptake system for dietary alkaloids in poison frogs (Dendrobatidae)
John W. Daly,Sherrie Secunda,H. M. Garraffo,Thomas F. Spande,Anthony. Wisnieski,John F. Cover +5 more
TL;DR: The skin of poison frogs contains a wide variety of alkaloids that presumably serve a defensive role, and an alkaloid uptake system provides a means of maintaining skin alkaloidal levels and suggests that some if not all such 'dendrobatid alkal steroids' may have a dietary origin.
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N6,9-disubstituted adenines: potent, selective antagonists at the A1 adenosine receptor.
TL;DR: The present study assessed the effect of N6 and N-9 substituents on the binding of adenines to the A1 and A2 receptors of rat brain cortex and striatum and also on the antagonism of the A2 receptor mediated stimulation of the adenylate cyclase of PC12 cells by N-ethyladenosine-5'-uronamide.
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Variability in alkaloid profiles in neotropical poison frogs (Dendrobatidae): genetic versus environmental determinants.
John W. Daly,Sherrie Secunda,H. Martin Garraffo,Thomas F. Spande,Anthony. Wisnieski,Charles Nishihira,John F. Cover +6 more
TL;DR: The genetic, environmental and dietary determinants of alkaloid profiles in dendrobatid frogs remain obscure, in particular the underlying cause for total absence in terrarium-reared frogs.
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Sulfur-containing 1,3-dialkylxanthine derivatives as selective antagonists at A1-adenosine receptors
Kenneth A. Jacobson,Leonidas Kiriasis,Suzanne Barone,Barton James Bradbury,Udai Kammula,Jean Michel Campagne,Sherrie Secunda,John W. Daly,John L. Neumeyer,Wolfgang Pfleiderer +9 more
TL;DR: Sulfur-containing analogues of 8-substituted xanthines were prepared in an effort to increase selectivity or potency as antagonists at adenosine receptors, and 2-Thio-8-aryl derivatives tended to be more potent at A2 receptors than the oxygen analogue.
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Pumiliotoxin alkaloids: a new class of sodium channel agents.
John W. Daly,Fabian Gusovsky,E. T. McNeal,Sherrie Secunda,Maureen Bell,Cyrus R. Creveling,Yukio Nishizawa,Larry E. Overman,Matthew J. Sharp,Daniel P. Rossignol +9 more
TL;DR: It appears likely that some "inactive" congeners bind to the PTX-B binding site, but do not activate sodium channels, since pumiliotoxins, unlike local anesthetics, had little or no effect on binding of [3H]batrachotoxinin A benzoate to sodium channels.